Project Manager; PMI Certified – Software Medical Device; SaMD

Project Manager (PMI Certified) – Software as a Medical Device (SaMD)

• Remote
• $80,000 - $110,000 per year

About Prenosis

Prenosis Inc. is an artificial intelligence company pioneering precision medicine in acute care. Our Immunix™ precision medicine platform drives the development of precision products and enables real‑time delivery of optimal therapy. We've created and validated the first FDA-authorized AI biomarker for sepsis, the Sepsis Immuno Score™.

At Prenosis, we:

Disrupt with evidence

Excel with integrity

Go far together

Our staff collectively defined these corporate values to demonstrate how our teams contribute to meaningful and authentic change in U.S. healthcare. We value our diverse talent, strive to foster a culture of continuous learning, and aim to maintain a feeling of belonging and shared sense of purpose.

Prenosis is headquartered in Chicago Illinois and generally operates on Central Time Zone.

Prenosis is seeking a PMI‑certified Project Manager with strong experience leading projects in FDA‑regulated SaMD environments. The ideal candidate brings disciplined project leadership, a solid understanding of medical device regulatory requirements, and the ability to coordinate highly technical, cross‑functional teams.

You will drive successful execution of software products used for processing clinical data, executing AI biomarkers, and enabling research within hospital environments, ensuring delivery on time, within scope, and in compliance with quality and regulatory standards such as FDA 21 CFR Part 820, IEC 62304, ISO 14971, and ISO 13485.

Responsibilities

Lead end‑to‑end planning and execution of SaMD development projects, including scope definition, scheduling, budgeting, resource planning, project risk management, and project change control.

Work closely with Product Management, Engineering, R&D, Data Science, Quality, and Regulatory teams to build, manage, and maintain comprehensive project plans that support platform development for clinical data processing, AI biomarker execution, and hospital‑based research workflows.

Manage multidisciplinary project teams (Software Engineering, QA/RA, Clinical, Cybersecurity, Dev Ops, Data Science) to ensure timely and coordinated delivery.

Develop and maintain project documentation including project charters, timelines, communication plans, decision logs, and dashboards.

Coordinate stage‑gate reviews and support alignment with design control requirements across the full development lifecycle.

Ensure that all project activities meet applicable safety, quality, and regulatory standards.

Regulatory & Quality Compliance

Support adherence to 21 CFR 820, ISO 13485, IEC 62304, ISO 14971, and internal SOPs throughout the development lifecycle.

Support regulatory submissions (including 510(k), De Novo, PMA) through planning, documentation readiness, and cross‑functional coordination.

Communication & Stakeholder Management

Serve as the central point of communication for project status, timelines, risks, and dependencies.

Deliver clear executive summaries, traceable status reports, and KPI‑driven progress updates.

Coordinate effectively with internal teams, external partners, hospital collaborators, and vendors.

Manage expectations through transparent communication and data‑driven forecasting.

Proactively identify, assess, and mitigate project risks through structured risk management processes.

Work with functional leaders to forecast resource needs, identify gaps, and support staffing planning.

Ensure platform development aligns with cybersecurity, privacy, usability, interoperability, and post‑market requirements.

Support Supplier Quality compliance by ensuring vendor management aligns with internal procedures.

Expected frequency and duration of travel:
Once per quarter

• PMI certification required (PMP, PgMP, or PMI‑ACP).
• Bachelor’s degree in Engineering, Computer Science, Life Sciences, or a related field (Master’s preferred).
• 5+ years of project management experience in a regulated medical device or healthcare technology setting.
• Hands‑on experience managing SaMD projects, including design control,…